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Quaternary containing

When a low foaming cleaner is desired, inclusion of alkoxylated mono alkyl quaternary salts is useful. Such quaternaries, containing both ethoxyl and propoxyl moieties, are effective [75]. [Pg.164]

By far the largest (46% of the total amine market) use of f was in fabric softeners ( quaternary ammonium compounds). Predominantly used were di-methyldialkylammonium chloride and the corresponding methyl sulfate. The alkyl is hydrogenated tallow. The volinne of f. in this area is reduced substantially since modem ester quats (->qtiatem-ary ammonium compounds) need no f Other quaternaries contain hydroxyethyl- or imidazolinium structures. Dispersions containing 5-7% f. are used in rinse cycles of household and commercial laundry machines, and 0.1-0.2% remains on the fabric. In drying cycles, the softeners are applied to the substrate (paper, wovens and nonwovens as well as foam pads). [Pg.104]

Temary and quaternary semiconductors are theoretically described by the virtual crystal approximation (VGA) [7], Within the VGA, ternary alloys with the composition AB are considered to contain two sublattices. One of them is occupied only by atoms A, the other is occupied by atoms B or G. The second sublattice consists of virtual atoms, represented by a weighted average of atoms B and G. Many physical properties of ternary alloys are then expressed as weighted linear combinations of the corresponding properties of the two binary compounds. For example, the lattice constant d dependence on composition is written as ... [Pg.2880]

A major difficulty with the Diels-Alder reaction is its sensitivity to sterical hindrance. Tri- and tetrasubstituted olefins or dienes with bulky substituents at the terminal carbons react only very slowly. Therefore bicyclic compounds with polar reactions are more suitable for such target molecules, e.g. steroids. There exist, however, several exceptions, e. g. a reaction of a tetrasubstituted alkene with a 1,1-disubstituted diene to produce a cyclohexene intermediate containing three contiguous quaternary carbon atoms (S. Danishefsky, 1979). This reaction was assisted by large polarity differences between the electron rich diene and the electron deficient ene component. [Pg.86]

Ammonia can act as a nucleophile toward primary and some secondary alkyl halides to give primary alkylamines Yields tend to be modest because the primary amine IS itself a nucleophile and undergoes alkylation Alkylation of ammonia can lead to a mixture containing a primary amine a secondary amine a tertiary amine and a quaternary ammonium salt... [Pg.956]

Quantum (Section 13 1) The energy associated with a photon Quaternary ammonium salt (Section 22 1) Salt of the type R4N X The positively charged ion contains a nitrogen with a total of four organic substituents (any combination of alkyl and aryl groups)... [Pg.1292]

Quaternary ammonium exchangers contain —R4N+ groups which are strongly basic and completely dissociated in the OH form and the anion form. [Pg.1113]

The reactions are catalyzed by tertiary amines, quaternary ammonium salts, metal salts, and basic ion-exchange resins. The products are difficult to purify and generally contain low concentrations of acryhc acid and some diester which should be kept to a minimum since its presence leads to product instabihty and to polymer cross-linking. [Pg.156]

Temporary hair dye products usually are formulated at a neutral or slightly acidic pH. Besides the dyes, the formulations may contain a small amount of a quaternary amine to neutralize the negative charge on the dyes, a fragrance, a small amount of a solvent or surfactant to solubilize the fragrance, and a preservative (Table 6). [Pg.456]

Heterogeneous Catalysis. The main discovery of the 1980s was the use of titanium sihcaUte (TS-1) a synthetic zeoHte from the ZSM family containing no aluminum and where some titanium atoms replace siUcon atoms in the crystalline system (Ti/Si = 5%) (33). This zeoHte can be obtained by the hydrolysis of a siUcate and an alkyl titanate in the presence of quaternary ammonium hydroxide followed by heating to 170°C. Mainly studies have been devoted to the stmcture of TS-1 and its behavior toward H2O2 (34). The oxidation properties of the couple H2O2/TS-I have been extensively developed in... [Pg.488]

The cationic acrylamide polymers may contain either tertiary amine or quaternary ammonium groups. Because of their positive charge, they are self-retaining on pulp fibers therefore, they can be used effectively in nonalum systems. [Pg.19]

A great number of different heterocycHc residues have been used as the terminal groups of PMDs. Examples appear throughout this article. PMDs containing residues with quaternary nitrogen atoms are traditionally called cyanine dyes (qv). [Pg.489]

Several of the Al—Li alloys developed in the 1980s contain both magnesium and copper. No quaternary Al—Cu—Li—Mg phase has been found in the alloys. The S -phase in addition to 5 and provides precipitation hardening. [Pg.119]

Ethylene oxide adds to the bis(2-hydtoxyethyl) teitiaiy amine in a random fashion where x y y = n y2. Ethoxylated amines, varying from strongly cationic to very weakly cationic in character, are available containing up to 50 mol of ethylene oxide/mol of amine. Ethyoxylated fatty amine quaternaries, cationic surfactants (both chloride from methyl chloride and acetate from acetic acid), ate also available. [Pg.219]

Higher order aUphatic quaternary compounds, where one of the alkyl groups contains - 10 carbon atoms, exhibit surface-active properties (167). These compounds compose a subclass of a more general class of compounds known as cationic surfactants (qv). These have physical properties such as substantivity and aggregation ia polar media (168) that give rise to many practical appHcations. In some cases the ammonium compounds are referred to as iaverse soaps because the charge on the organic portion of the molecule is cationic rather than anionic. [Pg.377]

There are two reasons why the concentration of quaternaries is beheved to remain at a low level in sewage treatment systems. First, quaternaries appear to bind anionic compounds and thus are effectively removed from wastewater by producing stable, lower toxicity compounds (205). Anionic compounds are present in sewer systems at significantly higher concentrations than are cations (202). Second, the nature of how most quaternaries are used ensures that their concentrations in wastewater treatment systems are always relatively low but steady. Consumer products such as fabric softeners, hair conditioners, and disinfectants contain only a small amount of quaternary compounds. This material is then diluted with large volumes of water during use. [Pg.379]

Fabric Softening. The use of quaternary surfactants as fabric softeners and static control agents can be broken down into three main household product types rinse cycle softeners tumble dryer sheets and detergents containing softeners, also known as softergents. Rinse cycle softeners... [Pg.382]

The most common catalysts in order of decreasing reactivity are haUdes of aluminum, boron, zinc, and kon (76). Alkali metals and thek alcoholates, amines, nitriles, and tetraalkylureas have been used (77—80). The largest commercial processes use a resin—catalyst system (81). Trichlorosilane refluxes in a bed of anion-exchange resin containing tertiary amino or quaternary ammonium groups. Contact time can be used to control disproportionation to dichlorosilane, monochlorosilane, or silane. [Pg.23]

Cationic Starches. The two general categories of commercial cationic starches are tertiary and quaternary aminoalkyl ethers. Tertiary aminoalkyl ethers are prepared by treating an alkaline starch dispersion with a tertiary amine containing a P-halogenated alkyl, 3-chloto-2-hydtoxyptopyl radical, or a 2,3-epoxypropyl group. Under these reaction conditions, starch ethers are formed that contain tertiary amine free bases. Treatment with acid easily produces the cationic form. Amines used in this reaction include 2-dimethylaminoethyl chloride, 2-diethylaminoethyl chloride, and A/-(2,3-epoxypropyl) diethylamine. Commercial preparation of low DS derivatives employ reaction times of 6—12 h at 40—45°C for complete reaction. The final product is filtered, washed, and dried. [Pg.345]

Quaternary ammonium alkyl ethers are prepared similarly an alkaline starch is reacted with a quaternary ammonium salt containing a 3-chloto-2-hydtoxyptopyl or 2,3-epoxyptopyl radical. Alternatively, such derivatives can be prepared by simple quaternization of tertiary aminoalkyl ethers by reaction with methyl iodide. Sulfonium (107) and phosphonium (108) starch salts have also been prepared and investigated. Further work has explained the synthesis of diethyl aminoethyl starch (109) as well as the production of cationic starches from the reaction of alkaline starch with... [Pg.345]


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See also in sourсe #XX -- [ Pg.54 ]




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